HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882848Generated: October 31, 2026
2-Iodoxybenzoic acid → HCID 86647370, compound
https://huagongshe.com/reaction/882848
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Iodoxybenzoic acid | HCID 108794 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86647371 | HCID 86647371 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86647370 | HCID 86647370 | — |
Reaction Steps
IBX (293 mg, 0.472 mmol) was added to a solution of (2R)-1-benzyl-N-(3-hydroxy-4-(methoxyamino)-4-oxo-1-phenylbutan-2-yl)-5-oxopyrrolidine-2-carboxamide (143 mg, 0.337 mmol) in DMSO (5 mL). After stiffing for 2 h more IBX (105 mg, 0.169 mmol) was added and the stirring continued overnight. The saturated aqueous NaHCO3 solution was added and the reaction mixture was diluted with water and DCM. The organic layer was separated and the aqueous layer was extracted with DCM. The combined organic layers were washed with water and dried (MgSO4). The crude product obtained was dissolved in a minimal amount of DCM and diethylether was added. The precipitate formed was isolated and dried in vacuo. The title compound was obtained as a colourless solid (12 mg, 8%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08236798B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-71923a5df56b4d36884389f96a92f22e |
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| Source note | uspto-grants-2012_08 |
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